Back to Search
Start Over
A novel stilbene-like compound that inhibits melanoma growth by regulating melanocyte differentiation and proliferation
- Source :
- Toxicology and applied pharmacology. 337
- Publication Year :
- 2017
-
Abstract
- Melanoma is the most aggressive form of skin cancer. Current challenges to melanoma therapy include the adverse effects from immunobiologics, resistance to drugs targeting the MAPK pathway, intricate interaction of many signal pathways, and cancer heterogeneity. Thus combinational therapy with drugs targeting multiple signaling pathways becomes a new promising therapy. Here, we report a family of stilbene-like compounds called A11 that can inhibit melanoma growth in both melanoma-forming zebrafish embryos and mouse melanoma cells. The growth inhibition by A11 is a result of mitosis reduction but not apoptosis enhancement. Meanwhile, A11 activates both MAPK and Akt signaling pathways. Many A11-treated mouse melanoma cells exhibit morphological changes and resemble normal melanocytes. Furthermore, we found that A11 causes down-regulation of melanocyte differentiation genes, including Pax3 and MITF. Together, our results suggest that A11 could be a new melanoma therapeutic agent by inhibiting melanocyte differentiation and proliferation.
- Subjects :
- 0301 basic medicine
MAPK/ERK pathway
Skin Neoplasms
Melanoma, Experimental
Mitosis
Antineoplastic Agents
Biology
Toxicology
03 medical and health sciences
chemistry.chemical_compound
Mice
Melanocyte differentiation
Cell Line, Tumor
Stilbenes
medicine
Animals
Humans
Protein kinase B
PAX3 Transcription Factor
Zebrafish
Cell Proliferation
Pharmacology
Microphthalmia-Associated Transcription Factor
Dose-Response Relationship, Drug
Melanoma
Cancer
Cell Differentiation
Zebrafish Proteins
medicine.disease
Microphthalmia-associated transcription factor
Gene Expression Regulation, Neoplastic
030104 developmental biology
chemistry
Immunology
Cancer research
Melanocytes
Signal transduction
Growth inhibition
Mitogen-Activated Protein Kinases
Proto-Oncogene Proteins c-akt
Signal Transduction
Subjects
Details
- ISSN :
- 10960333
- Volume :
- 337
- Database :
- OpenAIRE
- Journal :
- Toxicology and applied pharmacology
- Accession number :
- edsair.doi.dedup.....cb9e40e448dc8adb014f2cb8f807a9d5